Application 210136

Type
NDA
Sponsor
BRAEBURN PHARMA INC

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001BRIXADIBUPRENORPHINEINJECTION, EXTENDED RELEASE;SUBCUTANEOUS8MGNoNo
002BRIXADIBUPRENORPHINESOLUTION, EXTENDED RELEASE;SUBCUTANEOUS16MG/0.32ML (50MG/ML)YesYes
003BRIXADIBUPRENORPHINESOLUTION, EXTENDED RELEASE;SUBCUTANEOUS24MG/0.48ML (50MG/ML)YesYes
004BRIXADIBUPRENORPHINESOLUTION, EXTENDED RELEASE;SUBCUTANEOUS32MG/0.64ML (50MG/ML)YesYes
005BRIXADIBUPRENORPHINESOLUTION, EXTENDED RELEASE;SUBCUTANEOUS64MG/0.18ML (356MG/ML)YesYes
006BRIXADIBUPRENORPHINESOLUTION, EXTENDED RELEASE;SUBCUTANEOUS96MG/0.27ML (356MG/ML)YesYes
007BRIXADIBUPRENORPHINESOLUTION, EXTENDED RELEASE;SUBCUTANEOUS128MG/0.36ML (356MG/ML)YesYes

Documents#

Document, Submission type, Date table
DocumentSubmission typeDate
85203SUPPL 2026-03-02
84642SUPPL 2026-01-05
84585SUPPL 2025-12-29
83284SUPPL 2025-09-04
81895SUPPL 2025-04-09
77924ORIG 2024-03-25
77049SUPPL 2023-12-19
77044SUPPL 2023-12-19
74355ORIG 2023-11-06
74358ORIG 2023-05-23
74357ORIG 2023-05-23
57788ORIG2019-02-22